Daniel M. Snell
Impact in
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- Neuroinflammation and Neurodegeneration Mechanisms
- Parkinson's Disease Mechanisms and Treatments
Papers in
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- Epigenetics and DNA Methylation 2
- Genetics 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genetics and Neurodevelopmental Disorders 1
- Genetic Syndromes and Imprinting 1
- Animal Genetics and Reproduction 1
- Co-authors
- James M. A. Turner (4 shared papers)Katy Malpass (1 shared paper)Jennifer M. Pocock (1 shared paper)Kenneth J. Smith (1 shared paper)Arthur Roach (1 shared paper)Thomas M. Piers (1 shared paper)David A. Bechtold (1 shared paper)Woojin Lee (1 shared paper)
- Journals
- Nature (2 papers)Brain (1 paper)Developmental Cell (1 paper)Current Biology (1 paper)Cell Systems (1 paper)
- Partner nations
- United KingdomSwitzerlandSingapore
In The Last Decade
Daniel M. Snell
5 papers receiving 178 citations
Peers
Comparison fields: 5 of 67
- Neurology 27
- Biological Psychiatry 6
- Developmental Neuroscience 8
- Genetics 49
- Cellular and Molecular Neuroscience 29
Countries citing papers authored by Daniel M. Snell
This map shows the geographic impact of Daniel M. Snell's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Daniel M. Snell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel M. Snell more than expected).
Fields of papers citing papers by Daniel M. Snell
This network shows the impact of papers produced by Daniel M. Snell. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Daniel M. Snell. The network helps show where Daniel M. Snell may publish in the future.
Co-authors
The 24 scholars most cited alongside Daniel M. Snell, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 76 | |
| 2 | 2013 | 67 | |
| 3 | 2021 | 21 | |
| 4 | 2024 | 11 | |
| 5 | 2025 | 4 | |
| 6 | 2025 | 0 | |
| 7 | 2025 | 0 |
About Daniel M. Snell
Daniel M. Snell is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Neurology and Aging, having authored 7 papers that have together received 179 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Epigenetics and DNA Methylation (2 papers), Neurogenesis and neuroplasticity mechanisms (1 paper), Genetics and Neurodevelopmental Disorders (1 paper), Genetic Syndromes and Imprinting (1 paper), Animal Genetics and Reproduction (1 paper), T-cell and B-cell Immunology (1 paper) and Genetics, Aging, and Longevity in Model Organisms (1 paper). The work is most often cited by research in Neurology (27 citations), Biological Psychiatry (6 citations), Developmental Neuroscience (8 citations), Genetics (49 citations) and Cellular and Molecular Neuroscience (29 citations). Daniel M. Snell has collaborated with scholars based in United Kingdom, Switzerland and Singapore. Frequent co-authors include James M. A. Turner, Katy Malpass, Jennifer M. Pocock, Kenneth J. Smith, Arthur Roach, Thomas M. Piers, David A. Bechtold, Woojin Lee, James Briscoe and Rory J. Maizels. Their work appears in journals such as Nature, Brain, Developmental Cell, Current Biology and Cell Systems.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.